Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)

Research output: Contribution to journalLetter

1 Citation (Scopus)
Original languageEnglish
Pages (from-to)147-149
Number of pages3
JournalJournal of the Neurological Sciences
Volume368
DOIs
Publication statusPublished - Sep 15 2016

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Ubiquitin-Protein Ligases
Parkinson Disease
Differential Diagnosis
Phenotype
Mutation
Genes

Keywords

  • Homozygotic exon 3 deletion
  • PARK2
  • Parkinson's disease

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

@article{b1e7674402ce4dd3b1247480cbfce489,
title = "Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)",
keywords = "Homozygotic exon 3 deletion, PARK2, Parkinson's disease",
author = "Kota Sato and Toru Yamashita and Noriko Hatanaka and Mami Takemoto and Nozomi Hishikawa and Yasuyuki Ohta and Koji Abe",
year = "2016",
month = "9",
day = "15",
doi = "10.1016/j.jns.2016.07.004",
language = "English",
volume = "368",
pages = "147--149",
journal = "Journal of the Neurological Sciences",
issn = "0022-510X",
publisher = "Elsevier",

}

TY - JOUR

T1 - Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)

AU - Sato, Kota

AU - Yamashita, Toru

AU - Hatanaka, Noriko

AU - Takemoto, Mami

AU - Hishikawa, Nozomi

AU - Ohta, Yasuyuki

AU - Abe, Koji

PY - 2016/9/15

Y1 - 2016/9/15

KW - Homozygotic exon 3 deletion

KW - PARK2

KW - Parkinson's disease

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UR - http://www.scopus.com/inward/citedby.url?scp=84979071819&partnerID=8YFLogxK

U2 - 10.1016/j.jns.2016.07.004

DO - 10.1016/j.jns.2016.07.004

M3 - Letter

VL - 368

SP - 147

EP - 149

JO - Journal of the Neurological Sciences

JF - Journal of the Neurological Sciences

SN - 0022-510X

ER -